The ECG showed an electrocardiographic pattern in which Brugada type 2 syndrome was reported and the patient was sent to a cardiac arrhythmia treatment center, where flecainide confirmed the diagnosis. Electrophysiological examination showed a low arrhythmia profile, and the patient was advised to avoid the consumption of certain drugs and drug abuse in patients with Brugada syndrome. Brugada syndrome is distinguished by fainting or sudden death based on the electro-cardio graphic outline of ST segment advancement in the normal heart, but on the precordial paths from V1 to V3 and the right bundle division block. Polymorphic ventricular tachycardia is caused by syncope and sudden death. These electrocardiographic symbols may appear during a ...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
peer reviewedThe Brugada syndrome, a genetically transmitted disease according to an autosomal mode ...
International audienceBrugada syndrome is a rare inherited arrhythmia syndrome leading to an increas...
Artículos originales[ES] El síndrome de Brugada es una cardiopatía genética y no estructural debida ...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
Brugada syndrome is characterized by specific electrocardiographic (ECG) findings such as right bund...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
Introduction. Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment eleva...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
12-lead surface ECG was suggestive of but not diagnostic of Brugada syndrome. An exercise stress tes...
Abstract Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed f...
The Brugada syndrome is an inherited channelopathy that alters the main transmembrane ion currents t...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
BACKGROUND Brugada syndrome, a disease burdened by elevated risk of sudden unexpected cardiac death,...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
peer reviewedThe Brugada syndrome, a genetically transmitted disease according to an autosomal mode ...
International audienceBrugada syndrome is a rare inherited arrhythmia syndrome leading to an increas...
Artículos originales[ES] El síndrome de Brugada es una cardiopatía genética y no estructural debida ...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
Brugada syndrome is characterized by specific electrocardiographic (ECG) findings such as right bund...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
Introduction. Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment eleva...
As a clinical entity the Brugada syndrome has existed since 1992 and has been associated with a high...
12-lead surface ECG was suggestive of but not diagnostic of Brugada syndrome. An exercise stress tes...
Abstract Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed f...
The Brugada syndrome is an inherited channelopathy that alters the main transmembrane ion currents t...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
BACKGROUND Brugada syndrome, a disease burdened by elevated risk of sudden unexpected cardiac death,...
In 1992, Brugada and Brugada described 8 patients with a history of aborted sudden death and a disti...
Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed from being ...
peer reviewedThe Brugada syndrome, a genetically transmitted disease according to an autosomal mode ...